CLCN1 Molecular Characterization in 19 South-Italian Patients With Dominant and Recessive Type of Myotonia Congenita by Chiara Orsini, Roberta Petillo, Paola D'Ambrosio, Manuela Ergoli, Esther Picillo, Marianna Scutifero, Luigia Passamano, Alessandro De Luca, Luisa Politano

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Anesthetic management of a patient with sodium-channel myotonia: a case report by Naohisa Matsumoto, Rei Nishimoto, Yoshikazu Matsuoka, Yoshimasa Takeda, Hiroshi Morimatsu

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Sodium Channel Myotonia Due to Novel Mutations in Domain I of Nav1.4 by Serena Pagliarani, Sabrina Lucchiari, Marina Scarlato, Elisa Redaelli, Anna Modoni, Francesca Magri, Barbara Fossati, Stefano C. Previtali, Valeria A. Sansone, Marzia Lecchi, Mauro Lo Monaco, Mauro Lo Monaco, Giovanni Meola, Giacomo P. Comi, Giacomo P. Comi

Subjects: “…myotonia…”
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Muscle channelopathies: A review by Bridget R. McGowan, Abigail N. Schwaede, Lenika De Simone, Vamshi K. Rao

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The Clinical, Myopathological, and Genetic Analysis of 20 Patients With Non-dystrophic Myotonia by Quanquan Wang, Quanquan Wang, Zhe Zhao, Hongrui Shen, Qi Bing, Nan Li, Jing Hu

Subjects: “…non-dystrophic myotonia…”
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Myotonia and myotonic discharges of dystrophic myotonia type 1 at the first decade onset: a literature review and data of the case series by S. A. Kurbatov, V. M. Kenis, M. V. Savina, I. S. Kleimenova, N. S. Priymak, Yu. V. Kryukov, A. A. Kokorina, N. V. Ryadninskaya, I. A. Kuznetsova, O. A. Shchagina, A. V. Poliakov

Subjects: “…dystrophic myotonia…”
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Possible role of SCN4A skeletal muscle mutation in apnea during seizure by Dilşad Türkdoğan, Emma Matthews, Sunay Usluer, Aslı Gündoğdu, Kayıhan Uluç, Roope Mannikko, Michael G. Hanna, Sanjay M. Sisodiya, Hande S. Çağlayan

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Schwartz Jampel syndrome responding positively to carbamazepine therapy: a case report and a novel mutation by Gürkan Gürbüz, Hatice Mutlu Albayrak

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Axonal Neuropathy with Neuromyotonia by J Gordon Millichap, John J Millichap

Subjects: “…clinical myotonia…”
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Electrodiagnostic findings in myotonic dystrophy: A study on 12 patients by Ahmet S. Burakgazi

Subjects: “…Myotonic dystrophy, Myotonia, NCS findings…”
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Anesthesia Experience in a Patient with Myotonia Congenita by Yeşim Cokay Abut, Serkan Şimşek, Seher Köse, Şenay Kırgezen, Kübra Bolat, Veysel Erden

Subjects: “…myotonia congenita…”
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Neonatal Episodic Laryngospasm Treated with Sodium Channel Blockers by J Gordon Millichap

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Neutral lipid storage disease with myopathy and myotonia associated to pathogenic variants on PNPLA2 and CLCN1 genes: case report by João Igor Dantas Landim, Ian Silva Ribeiro, Eduardo Braga Oliveira, Hermany Capistrano Freitas, Lara Albuquerque Brito, Isaac Holanda Mendes Maia, Daniel Gurgel Fernandes Távora, Cleonisio Leite Rodrigues

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Schwartz–Jampel syndrome is not related to malignant hyperthermia by Kohei Godai

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Cushing’s Myopathy in Dogs: Prevalence, Clinical Abnormalities, and Response to Treatment by Kate Hovious, Kayla Fowler, Michaela Beasly, Theresa E. Pancotto

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Myotonia congenita and myoadenylate deaminase deficiency: case report by Scola Rosana Herminia, Iwamoto Fabio Massaiti, Camargo Carlos Henrique, Arruda Walter Oleschko, Werneck Lineu Cesar

Subjects: “…myotonia congenita…”
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Schwartz–jampel syndrome: Clinical and diagnostic phenotype of a rare genetic disorder by Bhaskara P Shelley, U S Vinayaka

Subjects: “…Chondrodystrophic myotonia…”
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The role of surface electromyography in the assessment of myotonia in Parkinson's disease by LIU Zai‑chao, JIAO Yue, LI Juan, CHEN Xian‑wen

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Autosomal recessive myotonia congenita, a muscle channelopathy, presenting in Nigerian siblings: A report by Ikenna O Onwuekwe, Oluchi S Ekenze, Birinus Ezeala-Adikaibe

Subjects: “…myotonia congenita…”
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ClC-1 Chloride Channel: Inputs on the Structure–Function Relationship of Myotonia Congenita-Causing Mutations by Oscar Brenes, Michael Pusch, Fernando Morales

Subjects: “…myotonia…”
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